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Diffusing capacity of the lung for carbon monoxide: association with long-term outcomes after lung transplantation in a 20-year longitudinal study.
Darley, David Ross; Ma, Jin; Huszti, Ella; Ghany, Rasheed; Hutcheon, Michael; Chow, Chung-Wai; Tikkanen, Jussi; Keshavjee, Shaf; Singer, Lianne Gail; Martinu, Tereza.
Afiliación
  • Darley DR; Toronto Lung Transplant Program, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
  • Ma J; UNSW Medicine, St Vincent's Clinical School, University of New South Wales, Sydney, Australia.
  • Huszti E; Biostatistics Research Unit, University Health Network, Toronto, ON, Canada.
  • Ghany R; Biostatistics Research Unit, University Health Network, Toronto, ON, Canada.
  • Hutcheon M; Toronto Lung Transplant Program, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
  • Chow CW; Toronto Lung Transplant Program, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
  • Tikkanen J; Toronto Lung Transplant Program, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
  • Keshavjee S; Dept of Medicine, University of Toronto, Toronto, ON, Canada.
  • Singer LG; Toronto Lung Transplant Program, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
  • Martinu T; Toronto Lung Transplant Program, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
Eur Respir J ; 59(1)2022 01.
Article en En | MEDLINE | ID: mdl-34172463
ABSTRACT
RATIONALE The diffusing capacity of the lung for carbon monoxide corrected for haemoglobin (D LCOcor) measures gas movement across the alveolar-capillary interface. We hypothesised that D LCOcor is a sensitive measure of injurious allograft processes disrupting this interface.

OBJECTIVES:

To determine the prognostic significance of the D LCOcor trajectory on chronic lung allograft dysfunction (CLAD) and survival.

METHODS:

A retrospective analysis was conducted of all bilateral lung transplant recipients at a single centre, between January 1998 and January 2018, with one or more D LCOcor measurements. Low baseline D LCOcor was defined as the failure to achieve a D LCOcor >75% predicted. Drops in D LCOcor were defined as >15% below recent baseline.

RESULTS:

1259 out of 1492 lung transplant recipients were included. The median (range) time to peak D LCOcor was 354 (181-737) days and the mean±sd D LCOcor was 80.2±21.2% pred. Multivariable analysis demonstrated that low baseline D LCOcor was significantly associated with death (hazrd ratio (HR) 1.68, 95% CI 1.27-2.20; p<0.001). Low baseline D LCOcor was not independently associated with CLAD after adjustment for low baseline forced expiratory volume in 1 s or forced vital capacity. Any D LCOcor declines ≥15% were significantly associated with death, independent of concurrent spirometric decline. Lower percentage predicted D LCOcor values at CLAD onset were associated with shorter post-CLAD survival (HR 0.75 per 10%-unit change, p<0.01).

CONCLUSION:

Low baseline D LCOcor and post-transplant declines in D LCOcor were significantly associated with survival, independent of spirometric measurements. We propose that D LCOcor testing may allow identification of a subphenotype of baseline and chronic allograft dysfunction not captured by spirometry. There may be benefit in routine monitoring of D LCOcor after lung transplantation to identify patients at risk of poor outcomes.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trasplante de Pulmón / Disfunción Primaria del Injerto Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Eur Respir J Año: 2022 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Trasplante de Pulmón / Disfunción Primaria del Injerto Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Eur Respir J Año: 2022 Tipo del documento: Article País de afiliación: Canadá